Canonical Allele Identifier: CA406004756
Gene: BCKDHA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410741C>A , CM000681.2:g.41410741C>A GRCh38
NC_000019.9:g.41916646C>A , CM000681.1:g.41916646C>A GRCh37
NC_000019.8:g.46608486C>A NCBI36
NG_013004.1:g.17953C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.213C>A MANE Select ENSP00000269980.2:p.Asn71Lys
ENST00000269980.6:c.213C>A ENSP00000269980.2:p.Asn71Lys
ENST00000457836.6:c.147C>A ENSP00000416000.2:p.Asn49Lys
ENST00000538423.5:n.233C>A
ENST00000540732.3:c.315C>A ENSP00000443246.1:p.Asn105Lys
ENST00000541315.1:c.20C>A
ENST00000542943.5:c.213C>A ENSP00000440345.1:p.Asn71Lys
ENST00000595085.5:c.213C>A ENSP00000471150.2:p.Asn71Lys
ENST00000604424.1:n.455C>A
NM_000709.3:c.213C>A NP_000700.1:p.Asn71Lys
NM_001164783.1:c.213C>A NP_001158255.1:p.Asn71Lys
NM_000709.4:c.213C>A MANE Select NP_000700.1:p.Asn71Lys
NM_001164783.2:c.213C>A NP_001158255.1:p.Asn71Lys